Mes Program Lead

Johnson & Johnson Johnson & Johnson · Pharma · Gent, East Flanders, Belgium

Lead the delivery of MES (Manufacturing Execution System) related programs for CAR-T manufacturing sites, focusing on capacity expansion, operational alignment, and regulatory compliance. This role involves managing project governance, cross-functional coordination, and issue resolution to ensure life-saving products reach patients.

What you'd actually do

  1. Lead the end‑to‑end delivery of MES‑related programs, including significant process updates (batch records changes) and the design of new batch records.
  2. Develop, align, and maintain a comprehensive project plan covering scope, schedule, budget, and resource needs.
  3. Drive project governance, ensuring traceability of decisions, clear ownership, and timely escalation of risks.
  4. Act as the central communication hub between Operations, QA, engineering, and vendor partners.
  5. Lead cross‑functional problem‑solving to address deviations, delays, or scope changes affecting MES deliverables.

Skills

Required

  • 6+ years of relevant industry experience in manufacturing, digital systems, operations, or project management.
  • Proven experience managing projects in a regulated, fast-paced, or technology‑driven environment.
  • Strong project management skills, with ability to manage scope, schedule, budget, risks, and cross‑functional alignment.
  • Excellent communication and organizational skills; ability to simplify complexity and maintain stakeholder engagement.
  • Strong problem‑solving capabilities and ability to independently drive actions to completion.
  • Proven ability to lead without direct authority, fostering collaboration and decision‑making across functions.
  • Comfortable navigating ambiguity, adapting quickly to evolving priorities, and maintaining momentum in a dynamic environment.
  • Proactive, solution‑oriented, and able to bring clarity and structure in complex situations.
  • Fluent in spoken and written English

Nice to have

  • Prior exposure to MES, advanced therapies, electronic batch records, or digital manufacturing systems is highly preferred.
  • Experience in cell therapy, biologics, sterile operations, or other GxP manufacturing environments.
  • Project management certification (PMP, Prince2, Agile) is an asset.
  • Familiarity with validated/regulated system lifecycle management
  • knowledge of Dutch is a plus

What the JD emphasized

  • strong project leadership
  • communication
  • execution discipline
  • fast-paced, advanced therapy environment
  • regulated, fast-paced, or technology‑driven environment
  • GxP manufacturing environments